✂️ ⚡ Rapid haploid variant calling and core genome alignment
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Updated
Jul 19, 2024 - Perl
✂️ ⚡ Rapid haploid variant calling and core genome alignment
Rapid large-scale prokaryote pan genome analysis
Application of pan-genome for population
simuG: a general-purpose genome simulator
EDGE is a highly adaptable bioinformatics platform that allows laboratories to quickly analyze and interpret genomic sequence data.
Improve the quality of a denovo assembly by scaffolding and gap filling
Graph-based mapping of long sequences, noisy or HiFi.
A pipeline to select optimal markers for microbial phylogenomics and species tree estimation using the multispecies coalescent and concatenation approaches
Collection of scripts for bacterial genomics
CoGe (Comparative Genomics) Platform
Genome Annotation Without Nightmares
MTBseq is an automated pipeline for mapping, variant calling and detection of resistance mediating and phylogenetic variants from illumina whole genome sequence data of Mycobacterium tuberculosis complex isolates.
LRSDAY: Long-read Sequencing Data Analysis for Yeasts
Multilocus sequence typing by blast using the schemes from PubMLST
Identify phage regions in bacterial genomes for masking purposes
Toolkit for preparing genomes for submission to NCBI
starfish: a modular toolkit for giant mobile element annotation
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